ClinVar Miner

List of variants in gene DEPDC5 reported by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 68
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HGVS dbSNP gnomAD frequency
NM_001242896.3(DEPDC5):c.1323A>C (p.Thr441=) rs5998135 0.11421
NM_001242896.3(DEPDC5):c.2170+11G>A rs55645350 0.10718
NM_001242896.3(DEPDC5):c.885A>G (p.Gln295=) rs16989495 0.03316
NM_001242896.3(DEPDC5):c.364-10C>T rs116263417 0.03313
NM_001242896.3(DEPDC5):c.1922C>T (p.Ala641Val) rs16989528 0.02752
NM_001242896.3(DEPDC5):c.1095T>C (p.Asp365=) rs79070552 0.02578
NM_001242896.3(DEPDC5):c.3358A>G (p.Met1120Val) rs61731662 0.02356
NM_001242896.3(DEPDC5):c.1165C>T (p.Arg389Cys) rs41311139 0.01988
NM_001242896.3(DEPDC5):c.4512C>T (p.His1504=) rs146449468 0.01383
NM_001242896.3(DEPDC5):c.2481G>A (p.Pro827=) rs61731664 0.01330
NM_001242896.3(DEPDC5):c.2742G>A (p.Glu914=) rs118001924 0.01176
NM_001242896.3(DEPDC5):c.2020C>T (p.Arg674Cys) rs181347577 0.00218
NM_001242896.3(DEPDC5):c.3265-3C>T rs371377906 0.00108
NM_001242896.3(DEPDC5):c.262A>G (p.Asn88Asp) rs144712084 0.00103
NM_001242896.3(DEPDC5):c.1330G>A (p.Gly444Arg) rs201394709 0.00071
NM_001242896.3(DEPDC5):c.3567A>G (p.Thr1189=) rs142197878 0.00063
NM_001242896.3(DEPDC5):c.1525C>T (p.Arg509Cys) rs202083639 0.00049
NM_001242896.3(DEPDC5):c.3092C>A (p.Pro1031His) rs376744360 0.00041
NM_001242896.3(DEPDC5):c.3805+10G>A rs201608608 0.00041
NM_001242896.3(DEPDC5):c.4683C>T (p.Ser1561=) rs370189053 0.00036
NM_001242896.3(DEPDC5):c.363+6_363+7del rs748242785 0.00027
NM_001242896.3(DEPDC5):c.3312G>A (p.Ser1104=) rs759169213 0.00024
NM_001242896.3(DEPDC5):c.161A>C (p.Gln54Pro) rs201312113 0.00019
NM_001242896.3(DEPDC5):c.2784C>T (p.Ala928=) rs201146392 0.00011
NM_001242896.3(DEPDC5):c.946+10G>C rs367917127 0.00011
NM_001242896.3(DEPDC5):c.4733A>G (p.Asp1578Gly) rs201347461 0.00009
NM_001242896.3(DEPDC5):c.2576C>T (p.Thr859Met) rs200744555 0.00007
NM_001242896.3(DEPDC5):c.2004A>G (p.Gly668=) rs374037144 0.00003
NM_001242896.3(DEPDC5):c.2619G>A (p.Thr873=) rs371442017 0.00003
NM_001242896.3(DEPDC5):c.3461C>T (p.Ser1154Phe) rs578244490 0.00003
NM_001242896.3(DEPDC5):c.871+9T>C rs373471598 0.00003
NM_001242896.3(DEPDC5):c.1960T>C (p.Ser654Pro) rs774477005 0.00002
NM_001242896.3(DEPDC5):c.2006+3G>A rs752184633 0.00002
NM_001242896.3(DEPDC5):c.138T>A (p.Asp46Glu) rs535630975 0.00001
NM_001242896.3(DEPDC5):c.1936A>G (p.Ser646Gly) rs377294383 0.00001
NM_001242896.3(DEPDC5):c.2527C>T (p.Arg843Ter) rs541024038 0.00001
NM_001242896.3(DEPDC5):c.3202G>A (p.Ala1068Thr) rs763158282 0.00001
NM_001242896.3(DEPDC5):c.*14_*15insAGGGTTAGAAGGCTGCACC rs566255762
NM_001242896.3(DEPDC5):c.1148A>G (p.His383Arg)
NM_001242896.3(DEPDC5):c.1159G>A (p.Ala387Thr)
NM_001242896.3(DEPDC5):c.1218-5del rs758572377
NM_001242896.3(DEPDC5):c.1300A>G (p.Lys434Glu)
NM_001242896.3(DEPDC5):c.147-10T>G rs1168103303
NM_001242896.3(DEPDC5):c.1666+189_1666+195del
NM_001242896.3(DEPDC5):c.1666+194_1666+195del rs10712869
NM_001242896.3(DEPDC5):c.1666+194_1666+195dup
NM_001242896.3(DEPDC5):c.1811C>T (p.Ser604Phe)
NM_001242896.3(DEPDC5):c.1866T>C (p.Pro622=)
NM_001242896.3(DEPDC5):c.2010C>T (p.His670=)
NM_001242896.3(DEPDC5):c.2049G>A (p.Leu683=) rs2148830090
NM_001242896.3(DEPDC5):c.2055C>A (p.Phe685Leu) rs61731667
NM_001242896.3(DEPDC5):c.2170+8G>C
NM_001242896.3(DEPDC5):c.2515G>A (p.Gly839Ser)
NM_001242896.3(DEPDC5):c.2521G>T (p.Val841Leu)
NM_001242896.3(DEPDC5):c.2768A>G (p.Gln923Arg)
NM_001242896.3(DEPDC5):c.3341A>T (p.Asp1114Val)
NM_001242896.3(DEPDC5):c.3486-5dup rs1555914747
NM_001242896.3(DEPDC5):c.3571G>A (p.Val1191Ile)
NM_001242896.3(DEPDC5):c.364-1G>C
NM_001242896.3(DEPDC5):c.364-9T>A
NM_001242896.3(DEPDC5):c.3805G>A (p.Val1269Met)
NM_001242896.3(DEPDC5):c.4078G>A (p.Val1360Met)
NM_001242896.3(DEPDC5):c.414-7C>T
NM_001242896.3(DEPDC5):c.4203+5G>A rs1569224557
NM_001242896.3(DEPDC5):c.4519+6G>A
NM_001242896.3(DEPDC5):c.4746C>T (p.Asn1582=)
NM_001242896.3(DEPDC5):c.71T>G (p.Val24Gly) rs572660873
NM_001242896.3(DEPDC5):c.767+10G>C

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